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What is Documents and Records about?

The document outlines the various categories of records and documents in the pharmaceutical industry, including primary documents, procedures, subsidiary documents, and quality control documents. It details commonly used documents such as quality manuals, SOPs, and batch records, as well as the importance of proper documentation in ensuring compliance with cGMP and regulatory standards. Documentation serves as evidence of manufacturing activities, aids in clarity and planning, and is essential for quality m

Author

Kavitha Seervi

Language

EN